【発表論文】

Sato, A., Kishida, S., Tanaka, T., Kikuchi, A., Kodama, T., Asashima,, M., and Nishinakamura, R. Sall1, a causative gene for Townes-Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin. Biochem. Biophys. Res. Commun, in press.

Takasato, M., Osafune, K., Matsumoto, Y., Kataoka, Y., Yoshida, N., Meguro, H., Aburatani, H., Asashima, M., Nishinakamura, R. Identification of kidney mesenchymal genes by a combination of microarray analysis and Sall1-GFP knockin mice. Mech Dev. 121 (6):547-557, 2004

Nakayama N, Han CY, Cam L, Lee JI, Pretorius J, Fisher S, Rosenfeld R, Scully S, Nishinakamura R, Duryea D, Van G, Bolon B, Yokota T, Zhang K. A novel chordin-like BMP inhibitor, CHL2, expressed preferentially in chondrocytes of developing cartilage and osteoarthritic joint cartilage. Development. 2004; 131(1): 229-240.

Nishinakamura, R. Kidney development conserverd overspecies:essential roles of Sall1. Semin. Cell Dev. Biol. 14 (4):241-247, 2003

Sato, A., Matsumoto, Y., Koide, U., Kataoka, Y., Yoshida, N,. Yokota, T., Asashima, M., and Nishinakamura, R. Zinc finger protein Sall2 is not essential for embryonic and kidney development. Mol. Cell. Biol. 23 (1):62-69, 2003

Osafune, K., Nishinakamura, R., Komazaki, S., and Asashima, M. In vitro induction of the pronephric duct in Xenopus explants. Dev. Growth. Differ. 44 (2):161-167, 2002

Nishinakamura, R., Matsumoto, Y., Nakao, K., Nakamura, K., Sato, A., Copeland, NG., Gilbert, DJ, Jenkins, NA., Scully, S., Lacey, DL., Katsuki, M., Asashima, M., and Yokota, T. Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development . Development 128: 3105-3115, 2001

Nakayama, N., Han, C., Nishinakamura, R., Scully, S., He, C., Zeni, L., Yamane, H., Chang, D., Yu, D., Yokota, T., and Wen, D. A novel chordin-like protein inhibitor for bone morphogenetic proteins expressed preferentially in mesenchymal cell lineages. Dev. Biol. 232:372-387, 2001.

Sato, A., Asashima, M., Yokota, T. and Nishinakamura, R. Cloning and expression pattern of a Xenopus pronephros-specific gene, XSMP-30. Mech Dev. 92:273-275, 2000

Tomida, M., Heike, T., and Yokota, T. Cytoplasmic domains of the leukemia inhibitory factor receptor required for STAT3 activation, differentiation, andgrowth arrest of myeloid leukemic cells. Blood, 93: 1934-1941, 1999.

Matsuda, T., Nakamura, T., Nakao, K., Arai, T., Katsuki, M,. Heike, T. and Yokota, T. STAT3 activation is sufficient to maintain an undifferentiated state of mouse embryonic stem cells. EMBO J, 18:4261-4269, 1999.

Matsuzaki, K., Katayama, K., Takahashi, Y., Nakamura, I., Udagawa, N., Tsurukai, T., Nishinakamura, R., Toyama, Y., Yabe, Y., Hori, M., Takahashi, N., and Suda, T. Human osteoclast-like cells are formed from peripheral blood mononuclear cells in a coculture with SaOS-2 cells transfected with the parathyroid hormone (PTH)/PTH-related protein receptor gene. Endocrinology 140(2):925-932, 1999.

Takagi, M., Nakamura, T., Sawada, T., Kaneko, A., Nozaki-Ukai, M., Nakahata, T., Yokota, T. and Heike, T. Chimeric cytokine receptor can transduce expansion signals in interleukin 6 receptor alpha (IL-6Ralpha)-, IL-11Ralpha-,and gp130-low to -negative primitive hematopoietic progenitors. Mol Biol Cell. 10:3633-3642, 1999.

Onuma, Y., Nishinakamura, R., Takahashi, S., Yokota, T. and Asashima, M. Molecular cloning of a novel Xenopus spalt gene (Xsal-3). Biochem Biophys Res Commun. 264:151-156, 1999.

Nishinakamura, R., Matsumoto, Y., Matsuda, T., Ariizumi, T., Heike, T., Asashima, M. and Yokota, T. Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4. Dev Biol. 216:481-490, 1999.

Nishinakamura, R., Matsumoto, Y., Uochi, T., Asashima, M., and Yokota, T. Xenopus FK 506-binding protein homolog induces a secondary axis in frog embryos, which is inhibited by coexisting BMP 4 signaling. Biochem. Biophys. Res. Commun. 239:585-591,1997.

Dirksen, U., Nishinakamura, R., Groneck, P., Hattenhorst, U., Nogee, L., Murray, R., and Burdach, S. Human pulmonary alveolar proteinosis associated with a defect in GM-CSF/IL-3/IL-5 receptor common βchain expression. J. Clin. Invest. 100:2211-2217, 1997.

Cooke, K.R., Nishinakamura, R., Martin, T.R., Kobzik, L., Brewer, J., Whitsett, J.A., Bungard, D., Murray, R., and Ferrara, J.L. Persistence of pulmonary pathology and abnormal lung function in IL-3/GM-CSF/IL-5 βc receptor-deficient mice despite correction of alveolar proteinosis after BMT. Bone Marrow Transplant. 20:657-662, 1997.

Mocci, S., Dalrymple, S.A., Nishinakamura, R., and Murray, R. The cytokine stew and innate resistance to L. monocytogenes. Immunol. Rev. 158:107-114, 1997.

Miyajima, A., Kinoshita, T., Wakao, H., Hara, T., Yoshimura, A., Nishinakamura, R., Murray, R., and Mui, A. Signal transduction by the GM-CSF, IL-3 and IL-5 receptors. Leukemia, Suppl. 3:418-422, 1997.

Nishinakamura, R., Wiler, R., Dirksen, U., Morikawa, Y., Arai, K., Miyajima, A., Burdach, S., and Murray, R. The pulmonary alveolar proteinosis in granulocyte macrophage colony-stimulating factor/ interleukins 3/5 βc receptor-deficient mice is reversed by bone marrow transplantation. J. Exp. Med. 183:2657-2662, 1996.

Nishinakamura, R., Miyajima, A., Mee, P.J., Tybulewicz, V.L.J., and Murray, R. Hematopoiesis in mice lacking the entire granulocyte-macrophage colony-stimulating factor/interleukin-3/interleukin-5 functions. Blood 88:2458-2464, 1996.

Nishinakamura, R., Burdach, S., Dirksen, U., and Murray, R. The in vivo role of the receptors for IL-3, GM-CSF, and IL-5 (βc andβIL3). Contemporary Immunology: Cytokine Knockouts. Humana Press Inc. 419-434, 1995.

Nishinakamura, R., Nakayama, N., Hirabayashi, Y., Inoue, T., Aud, D., McNeil, T., Azuma, S., Yoshida, S., Toyoda, Y., Arai, K., Miyajima, A., and Murry, R. Mice deficient for the IL-3/GM-CSF/IL-5 βc receptor exhibit lung pathology and impaired immune response, while βIL3 receptor-deficient mice are normal. Immunity 2:211-222, 1995.

     

【和文総説】

原田美貴、西中村隆一 腎発生を制御する遺伝子群. 腎臓ナビゲーター. 印刷中

原田美貴、西中村隆一 泌尿器系形成. 発生生物学がわかる. 羊土社.100-105, 2004

長船健二、西中村隆一 腎臓発生の分子機序. 小児外科.35:339-345,2003

長船健二、西中村隆一 腎臓の発生と再生医療. 最新医学. 58:719-729, 2003

西中村隆一 器官および臓器の特異的3次元構造の形成、維持に関わる遺伝的プログラム. 日本臨床. 61(3):370-374, 2003

西中村隆一 腎臓発生を制御する遺伝子群. Nephrology Frontier.1:24-29, 2002

西中村隆一 器官発生のメカニズム. 医学のあゆみ. 199(13):929-934, 2001

西中村隆一、横田崇 ES細胞による再生医療の現状. 「発生・分化・再生」生物の科学 遺伝別冊. 裳華房 13:130-136, 2001

西中村隆一、横田崇 腎臓の発生と分化−腎臓に幹細胞はあるか?. 幹細胞研究の最前線と再生医療への応用. 実験医学. 羊土社. 19(15):2021-2027, 2001

西中村隆一、松田孝彦、横田崇 ES細胞および初期発生におけるgp130/Stat3. サイトカインの新たな機能と生命現象. 実験医学. 羊土社. 18(15):73-80, 2000

高木峰生、平家俊男、横田崇 キメラレセプターを用いた造血幹細胞の増殖・分化機構の解析. 造血幹細胞をめぐる研究の新展開. 実験医学. 羊土社. 17(9):85-90, 1999

松田孝彦、平家俊男、横田崇 ES細胞の多分化能を維持するシグナル。シグナル伝達総集編。実験医学. 羊土社.17(14):210-218, 1999

     

     

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最終更新日 2004年5月26日